Tag | Content |
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EnhancerAtlas ID | HS042-16011 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr15:78911780-78913050 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH15I078619 | chr15 | 78911434 | 78912908 |
| Enhancer Sequence | GAAAGATGGC CAGTCCGCTC CCAGGGGCAG GGCCAACCAC GGTCGCCCAG GCCCAGGTCT 60 TCTACCTCCC AGCCTCCGGG AGAACACAGC CCAGGTCTGG GCCTCTCCTG CATTCCACCC 120 TGTAGGGGTG GCCACCAGCC CTCTTAGAAG CCAAGGCACT GTGTGACTCC CGTGATCTCG 180 TGTGACCCCC AGCTCTTGCT GATGCTGTCT TCATATCCTG ATGAAAGACT CTGACCTCTG 240 CAACCCTTGG GCACCCCTCT TTGTTCCTAA GCCACACCCC AGCACAAGTG AGGCATACCG 300 GGTCAGCTGT CTTCTGATTC CCACGTACAG ATCTGGGGGC AGCTTGGGGA AGCGGGAGGA 360 GAATCCTCTA GGAAGTTGAA TCCAACTTCC TCAGGTCTTG AAATAGGATT TTTCCTGCTC 420 CCCACTCTCC TTCCCCAGGA TGAAAGAAGG GTCCCAGGCA GGAGGTCGGT TGAGAGCGTA 480 TGGCGTTCTG AGTAGTGCAG GCCTCGGCAC CGAGGGCGGA AAGCGCTCTG AGCTCACAGC 540 CGCACGACAG ACCGCCGGCC TGGGCCCTCC AGGAATTCCC TGCAGCCTTG CCCGGTCCCC 600 GACTCTCGCT ACCCACCAGC CCTCCCAGGC ACCCAAGAGC CTCCCAGCGG CGGGCCAGGG 660 CCGGCTTCCC CCAGCAGGCT CCTCTGGAGA GCGGGAGGAA GACAGGAGGC GCTCTCCCGG 720 TGGAGGGTCC CTCAGCGACG CAGCCAGGAG CGCTAGGAGG CTACAACCGG AGGAGAGGCT 780 GGCGCTCCAG CTCCAGCCCC AGTCCCGAAG CGACTCCCCT CTTCCCGAGG TGGCCTTGGC 840 CAAGTCTTCA GCCATCTCCG TCAAATGAGG AGGTGGGCGG GATGCAGACG GTGGAGCGGG 900 AGGCTTGGGC GCGCCAGTTT GGGAGCCAGT GCGCGGGGCA GGGCGACGGG CAGCGCGGGG 960 ACGCGAATCC CCAACTCCTG CGCCCAAGAC GAAGGACCCG GTCTCGACCT CCCCATCACC 1020 CGGCGCGTAC CAGCGCCCGC TCAGTGACTC CCAGGTTTGG TGGTGGCTAG GGGTGGGAGG 1080 TGAGCCGAAA GGGAAAAAGC CACCCCACCC AAGTCGCCGC CGGGCTGGAG CCAGTCTGCG 1140 CGGGTTCCGA GTCCCCGGCG ACGGCGCCAG CCCTCTCCGC TCGCCCGCGC GGTGTTCTCG 1200 CCGGCAGCCC CTCCGGACCC CGCGCCCCTT CTCGGGCGCC CGTCCCTCCG GAGCCCTAAC 1260 GCCTGTGCGC 1270
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